Product Wiki · Recalls · Health Canada — Medical Devices

Remipack (2013-12-12) — recall 50787

Health Canada — Medical Devices · Canada · 2014-02-03 · Type I

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Agency
Health Canada — Medical Devices
Recall identifier
50787
Date of alert
2014-02-03
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Baxter has issued a product safety alert with respect to their flexible solution container (NaCl 0.9% I.V. bags) which is contained in the Remipack kits. Baxter flexible solution containers that have either a blue or neutral color administration port protector are affected. This safety alert is being issued to provide the following additional instruction, which in some cases, is not included on labeling for these products: do not use a flexible solution container if the administration port protector is not in place prior to use.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/remipack-2013-12-12

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